A rare, genetic syndromic intellectual disability characterized by developmental delay, mild to severe intellectual disability, facial features (bulbous nasal tip, and macroglossia, macrostomia, or open mouth appearance) and a wide spectrum of other nonspecific variable clinical features, such as cardiac defects. The disease is cardiac anomalies - developmental delay - facial dysmorphism syndrome (MONDO_0014773). Also known as: ASRAS, Asadollahi-Rauch syndrome, MED13L haploinsufficiency syndrome, MED13L syndrome, MED13L-related intellectual disability, MRFACD, developmental delay-facial dysmorphism syndrome due to MED13L deficiency, impaired intellectual development and distinctive facial features with or without cardiac defects.